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dc.contributor.authorATAMER, T
dc.contributor.authorKIRAC, K
dc.contributor.authorONAN, U
dc.contributor.authorSOYDINC, M
dc.contributor.authorSAGLAM, F
dc.date.accessioned2021-03-02T21:40:37Z
dc.date.available2021-03-02T21:40:37Z
dc.date.issued1995
dc.identifier.citationSAGLAM F., ATAMER T., ONAN U., SOYDINC M., KIRAC K., "INFANTILE GENETIC AGRANULOCYTOSIS (KOSTMANN TYPE) - A CASE-REPORT", JOURNAL OF PERIODONTOLOGY, cilt.66, sa.9, ss.808-810, 1995
dc.identifier.issn0022-3492
dc.identifier.otherav_084568c8-a2ad-4285-a795-d7b8de5cd474
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/11377
dc.identifier.urihttps://doi.org/10.1902/jop.1995.66.9.808
dc.description.abstractSEVERE PERIODONTITIS IN A PATIENT WITH INFANTILE genetic agranulocytosis (Kostmann syndrome) is presented. This rare syndrome is inherited as an autosomal recessive pattern and characterized by severe neutropenia. The periodontal status and treatment of the patient is described. It is concluded that periodontal therapy including scaling, root planing, soft tissue curettage, and the use of selected antimicrobial agents can be successful in this particular syndrome.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectDiş Hekimliği
dc.titleINFANTILE GENETIC AGRANULOCYTOSIS (KOSTMANN TYPE) - A CASE-REPORT
dc.typeMakale
dc.relation.journalJOURNAL OF PERIODONTOLOGY
dc.contributor.department, ,
dc.identifier.volume66
dc.identifier.issue9
dc.identifier.startpage808
dc.identifier.endpage810
dc.contributor.firstauthorID116588


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